Vanishing White Matter Disease with Mutations in EIF2B5 Gene
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[1] G. Scheper,et al. Vanishing White Matter Disease Associated With Ptosis and Myoclonic Seizures , 2011, Journal of child neurology.
[2] G. Scheper,et al. Leukoencephalopathy With Vanishing White Matter: A Review , 2010, Journal of neuropathology and experimental neurology.
[3] G. Scheper,et al. Vanishing White Matter , 2010 .
[4] V. Wong,et al. Vanishing White Matter Disease: The First Reported Chinese Patient , 2008, Journal of child neurology.
[5] H. Morizono,et al. Genetic and Clinical Heterogeneity in eIF2B-Related Disorder , 2008, Journal of child neurology.
[6] G. Scheper,et al. Vanishing white matter disease , 2006, The Lancet Neurology.
[7] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[8] Rune R. Frants,et al. Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter , 2001, Nature Genetics.
[9] K. Takeshita,et al. A Japanese girl with leukoencephalopathy with vanishing white matter , 2001, Brain and Development.
[10] Robert C. Wolpert,et al. A Review of the , 1985 .